FDA recall record

IBUPROFEN Children's Ibuprofen Oral Suspension, USP, 100 mg per 5mL, 4 FL OZ (120 mL) bottle recall — FDA D-0390-2026

Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.

Class IIclassification
D-0390-2026official record ID
Mar 25, 2026report date

Recall record at a glance

Official recordD-0390-2026
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSTRIDES PHARMA INC
Report dateMar 25, 2026
Recall initiation dateMar 2, 2026
Quantity89592 bottles
LocationBridgewater, NJ, United States

Official product description

Children's Ibuprofen Oral Suspension, USP, 100 mg per 5mL, 4 FL OZ (120 mL) bottle, Manufactured for: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, Made in India, NDC 51672-5321-8.

Why the product was recalled

Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.

Distribution information

U.S.A. Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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